BioWorld. Link to homepage.
BioWorld
BioWorld Science
BioWorld Asia
Data Snapshots
Biopharma
Medical technology
Infographics: Dynamic digital data analysis
Index insights
NME Digest
Special reports
Infographics: Dynamic digital data analysis
Trump administration impacts
Under threat: mRNA vaccine research
BioWorld at 35
Biopharma M&A scorecard
Bioworld 2025 review
BioWorld MedTech 2025 review
BioWorld Science 2025 review
Women's health
China's GLP-1 landscape
PFA re-energizes afib market
China CAR T
Alzheimer's disease
Coronavirus
More reports can be found here
BioWorld. Link to homepage.
Sign In
Sign Out
My Account
Subscribe
BioWorld - Thursday, February 19, 2026
Home
»
Topics
»
Regulatory
» EMA
EMA
RSS
Roche reports on third quarter of 2010
Nov. 18, 2010
EMA approves Cell Therapeutics' pediatric investigation plan for Pixuvri
Nov. 17, 2010
EMA orphan drug status for SBC-102 in LAL deficiency / News in Context
Nov. 17, 2010
EMA committee recommends orphan drug status for ThermoDox in primary liver cancer
Nov. 12, 2010
Schering-Plough Europe withdraws MAA for Zenhale
Nov. 11, 2010
MabThera approved in E.U. as maintenance treatment of follicular lymphoma
Nov. 4, 2010
Genta receives EMA advice for phase III tesetaxel trial in gastric cancer
Nov. 3, 2010
E.U. grants authorization for Ruconest in hereditary angioedema
Oct. 29, 2010
EMA recommends changes in prescribing information for Invirase
Oct. 26, 2010
CHMP recommends new indication for Bristol-Myers Squibb's Sprycel
Oct. 26, 2010
Previous
1
2
…
135
136
137
138
139
140
141
142
143
…
159
160
Next